• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance • Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans • Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate • Demonstrates diligence in protecting the confidentiality of each subject/patient • Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues • Assesses site processes as per the Clinical Monitoring/Site Management Plan (CMP/SMP) • Conducts Source Document Review of appropriate site source documents and medical records • Verifies required clinical data entered in the case report form (CRF) is accurate and complete • Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines • Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture • Verifies site compliance with electronic data capture requirements • May perform investigational product (IP) inventory, reconciliation and reviews storage and security • Verifies the IP has been dispensed and administered to subjects/patients according to the protocol • Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations • Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan • Supports subject/patient recruitment, retention and awareness strategies • For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met

• Contributing to the development and output of research and data tools that advance the Companys strategic goals and mission. • Providing research counsel and support to internal colleagues, grantees, and external stakeholders. • Actively contributing to the Companys research agenda to further empirical understanding of law school access, affordability, academic and bar success, and the value of legal education; • Assisting in management and maintenance of the Center's research and data tools, e.g., Analytix and XploreJD. • Organizing, structuring and cleaning data to permit for use to perform research and policy analysis. • Conducting basic statistical analyses using both internal and external data; supporting the production of visually appealing and easy to interpret tables and graphical displays of statistical results. • Advising and assisting colleagues, grantees, external researchers and consultants with research design, data analysis, data interpretation, and identifying and navigating higher education data sources. • Contributing to Company efforts to communicate findings to policy and practitioner audiences in succinct briefs, white papers, and reports. • Presenting at professional conferences; representing the Center at relevant industry conferences and events. • Assisting in the development and maintenance of a repository of research evidence and data that can support the Companys research objectives.

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects • Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded • Conduct study initiation visits (SIVs) • Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements

• Considered as the primary point of contact for the investigative site. • Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program. • Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol. • Advanced understanding of site engagement and ability to customize site engagement strategy for assigned studies. • Gather local/site insights and utilize site engagement tools to report/track progress and measure impact of that strategy. • Evaluate and ensure effective recruitment and retention techniques/plans based on patient disease journey. • Develop solid knowledge of therapeutic area, asset, and clinical landscape to enable successful patient recruitment. • Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting.